E90Q (p.Glu90Gln) variant of LHCGR (P22888)
E90Q (p.Glu90Gln) in LHCGR (P22888) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.60 / 1. The record also includes population frequency data and structural context.
E90Q (p.Glu90Gln) variant details
- p.Glu90Gln
- Ensembl rs2103621277
- Missense
- Variant Prioritization Score for Impact Estimate 0.599
- REVEL 0.50
- CADD 21.80
- PolyPhen-2 0.43
- SIFT 0.15
- Most common in the South Asian population (allele frequency 2.3e-05)
- Structural context available